Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list American Dental Technologies with 8 510(k) clearances. The most recent is a 510(k) clearance dated Apr 15, 2003: DIOLASE 980 D LASER SYSTEM.
| Apr 15, 2003 | DIOLASE 980 D LASER SYSTEMK023547 · GEX | 510(k) clearances |
| Oct 4, 2001 | PULSEMASTER ERBIUM DENTAL LASER SYSTEMK012127 · GEX | 510(k) clearances |
| Aug 13, 2001 | GULLIVER AND CLASSE AK012213 · EIA | 510(k) clearances |
| May 13, 1999 | PULSEMASTER DENTAL LASER SYSTEMK984486 · GEX | 510(k) clearances |
| Sep 19, 1997 | PULSEMASTER 1000 ST DENTAL LASER SYSTEMK972325 · GEX | 510(k) clearances |
| Mar 10, 1997 | PULSEMASTERK961269 · GEX | 510(k) clearances |
| Jun 3, 1996 | PULSEMASTERK961136 · GEX | 510(k) clearances |
| Aug 10, 1995 | PLASMA ARC CURING SYSTEMK952333 · EBF | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
